Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HMW2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043022 | ribosome binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 493 | 497 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 929 | 933 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.387 |
CLV_PCSK_FUR_1 | 732 | 736 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 712 | 714 | PF00082 | 0.175 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 712 | 714 | PF00082 | 0.175 |
CLV_PCSK_PC1ET2_1 | 734 | 736 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.610 |
CLV_PCSK_PC7_1 | 708 | 714 | PF00082 | 0.175 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.203 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 855 | 859 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 875 | 879 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 918 | 922 | PF00082 | 0.569 |
CLV_Separin_Metazoa | 342 | 346 | PF03568 | 0.347 |
CLV_Separin_Metazoa | 92 | 96 | PF03568 | 0.553 |
DEG_COP1_1 | 676 | 685 | PF00400 | 0.429 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.378 |
DEG_SPOP_SBC_1 | 936 | 940 | PF00917 | 0.475 |
DOC_CKS1_1 | 577 | 582 | PF01111 | 0.465 |
DOC_CYCLIN_yCln2_LP_2 | 644 | 647 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 171 | 178 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 201 | 210 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 608 | 617 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 65 | 75 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 732 | 742 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 837 | 844 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 608 | 615 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 67 | 75 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 608 | 616 | PF00069 | 0.312 |
DOC_PP1_RVXF_1 | 873 | 879 | PF00149 | 0.271 |
DOC_PP2B_LxvP_1 | 613 | 616 | PF13499 | 0.295 |
DOC_PP2B_LxvP_1 | 644 | 647 | PF13499 | 0.499 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 862 | 866 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 931 | 935 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 936 | 940 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.424 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 247 | 251 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 546 | 551 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 570 | 577 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 664 | 672 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 792 | 798 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 812 | 817 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 892 | 898 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 950 | 959 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 36 | 53 | PF00022 | 0.403 |
LIG_Actin_WH2_2 | 810 | 828 | PF00022 | 0.424 |
LIG_BIR_III_4 | 932 | 936 | PF00653 | 0.468 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.472 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.472 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.523 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.484 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.393 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.323 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.295 |
LIG_FHA_1 | 839 | 845 | PF00498 | 0.397 |
LIG_FHA_1 | 848 | 854 | PF00498 | 0.433 |
LIG_FHA_1 | 892 | 898 | PF00498 | 0.459 |
LIG_FHA_1 | 920 | 926 | PF00498 | 0.633 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.416 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.510 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.466 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.418 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.390 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.402 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.438 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.451 |
LIG_FHA_2 | 919 | 925 | PF00498 | 0.468 |
LIG_IRF3_LxIS_1 | 15 | 21 | PF10401 | 0.510 |
LIG_LIR_Gen_1 | 138 | 148 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 16 | 22 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 372 | 382 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 527 | 536 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 545 | 556 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 588 | 598 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 600 | 611 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 623 | 632 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 722 | 730 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 755 | 766 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 799 | 807 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 833 | 842 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 623 | 628 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 722 | 726 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 754 | 759 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 799 | 804 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 829 | 835 | PF02991 | 0.446 |
LIG_LYPXL_S_1 | 408 | 412 | PF13949 | 0.363 |
LIG_LYPXL_yS_3 | 386 | 389 | PF13949 | 0.413 |
LIG_LYPXL_yS_3 | 409 | 412 | PF13949 | 0.363 |
LIG_NRBOX | 843 | 849 | PF00104 | 0.435 |
LIG_NRBOX | 897 | 903 | PF00104 | 0.404 |
LIG_PCNA_PIPBox_1 | 482 | 491 | PF02747 | 0.376 |
LIG_PCNA_yPIPBox_3 | 190 | 200 | PF02747 | 0.267 |
LIG_PCNA_yPIPBox_3 | 45 | 59 | PF02747 | 0.376 |
LIG_PCNA_yPIPBox_3 | 633 | 642 | PF02747 | 0.408 |
LIG_SH2_CRK | 141 | 145 | PF00017 | 0.359 |
LIG_SH2_CRK | 197 | 201 | PF00017 | 0.259 |
LIG_SH2_CRK | 513 | 517 | PF00017 | 0.398 |
LIG_SH2_CRK | 625 | 629 | PF00017 | 0.526 |
LIG_SH2_CRK | 723 | 727 | PF00017 | 0.339 |
LIG_SH2_CRK | 835 | 839 | PF00017 | 0.437 |
LIG_SH2_GRB2like | 375 | 378 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 758 | 761 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 813 | 816 | PF00017 | 0.411 |
LIG_SH2_SRC | 347 | 350 | PF00017 | 0.402 |
LIG_SH2_SRC | 375 | 378 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 832 | 836 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.423 |
LIG_SH3_1 | 643 | 649 | PF00018 | 0.478 |
LIG_SH3_3 | 643 | 649 | PF00018 | 0.470 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.333 |
LIG_Sin3_3 | 529 | 536 | PF02671 | 0.391 |
LIG_Sin3_3 | 774 | 781 | PF02671 | 0.429 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 355 | 362 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 737 | 745 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 758 | 764 | PF11976 | 0.271 |
LIG_TRAF2_1 | 752 | 755 | PF00917 | 0.418 |
LIG_TYR_ITIM | 15 | 20 | PF00017 | 0.511 |
LIG_TYR_ITIM | 721 | 726 | PF00017 | 0.339 |
LIG_UBA3_1 | 637 | 643 | PF00899 | 0.455 |
LIG_UBA3_1 | 671 | 677 | PF00899 | 0.361 |
LIG_UBA3_1 | 739 | 747 | PF00899 | 0.368 |
LIG_UBA3_1 | 897 | 904 | PF00899 | 0.537 |
LIG_UBA3_1 | 93 | 102 | PF00899 | 0.494 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.516 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.478 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.581 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.575 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.478 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.272 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.437 |
MOD_CK1_1 | 830 | 836 | PF00069 | 0.528 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.399 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.690 |
MOD_CK1_1 | 984 | 990 | PF00069 | 0.792 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.411 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.529 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.535 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.460 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.281 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.402 |
MOD_CK2_1 | 816 | 822 | PF00069 | 0.379 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.462 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.404 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.415 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.413 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.367 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.483 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.410 |
MOD_GlcNHglycan | 864 | 867 | PF01048 | 0.381 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.598 |
MOD_GlcNHglycan | 932 | 936 | PF01048 | 0.661 |
MOD_GlcNHglycan | 941 | 944 | PF01048 | 0.706 |
MOD_GlcNHglycan | 947 | 950 | PF01048 | 0.762 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.469 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.461 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.478 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.439 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.315 |
MOD_GSK3_1 | 812 | 819 | PF00069 | 0.409 |
MOD_GSK3_1 | 888 | 895 | PF00069 | 0.397 |
MOD_GSK3_1 | 931 | 938 | PF00069 | 0.661 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.674 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.463 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.533 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.543 |
MOD_N-GLC_1 | 892 | 897 | PF02516 | 0.433 |
MOD_N-GLC_2 | 861 | 863 | PF02516 | 0.307 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.488 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.565 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.534 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.362 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.495 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.443 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.439 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.292 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.352 |
MOD_NEK2_1 | 793 | 798 | PF00069 | 0.379 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.393 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.467 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.402 |
MOD_NEK2_1 | 847 | 852 | PF00069 | 0.407 |
MOD_NEK2_1 | 888 | 893 | PF00069 | 0.453 |
MOD_NEK2_1 | 910 | 915 | PF00069 | 0.444 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.408 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.424 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.555 |
MOD_PIKK_1 | 799 | 805 | PF00454 | 0.545 |
MOD_PK_1 | 121 | 127 | PF00069 | 0.577 |
MOD_PK_1 | 546 | 552 | PF00069 | 0.397 |
MOD_PK_1 | 892 | 898 | PF00069 | 0.409 |
MOD_PKA_1 | 86 | 92 | PF00069 | 0.431 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.508 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.541 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.519 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.406 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.591 |
MOD_PKA_2 | 891 | 897 | PF00069 | 0.402 |
MOD_PKA_2 | 949 | 955 | PF00069 | 0.487 |
MOD_PKB_1 | 767 | 775 | PF00069 | 0.189 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.518 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.352 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.474 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.457 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.394 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.521 |
MOD_Plk_1 | 892 | 898 | PF00069 | 0.416 |
MOD_Plk_1 | 984 | 990 | PF00069 | 0.652 |
MOD_Plk_2-3 | 926 | 932 | PF00069 | 0.456 |
MOD_Plk_2-3 | 981 | 987 | PF00069 | 0.559 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.424 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.525 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.320 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.473 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.385 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.400 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.447 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.389 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.348 |
MOD_Plk_4 | 827 | 833 | PF00069 | 0.378 |
MOD_Plk_4 | 892 | 898 | PF00069 | 0.418 |
MOD_Plk_4 | 910 | 916 | PF00069 | 0.316 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.440 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.415 |
MOD_SUMO_for_1 | 359 | 362 | PF00179 | 0.371 |
MOD_SUMO_for_1 | 423 | 426 | PF00179 | 0.368 |
MOD_SUMO_for_1 | 702 | 705 | PF00179 | 0.301 |
MOD_SUMO_for_1 | 711 | 714 | PF00179 | 0.290 |
MOD_SUMO_rev_2 | 105 | 110 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 535 | 541 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 96 | 103 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_1 | 773 | 778 | PF01217 | 0.314 |
TRG_DiLeu_BaEn_1 | 962 | 967 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 789 | 794 | PF01217 | 0.353 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 723 | 726 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 758 | 761 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 813 | 816 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 835 | 838 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 767 | 770 | PF00400 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 6 | 10 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M4 | Leptomonas seymouri | 76% | 91% |
A0A0N0P521 | Leptomonas seymouri | 32% | 99% |
A0A0S4JES4 | Bodo saltans | 33% | 97% |
A0A0S4JKV4 | Bodo saltans | 44% | 96% |
A0A1X0NLE6 | Trypanosomatidae | 33% | 98% |
A0A1X0P5E9 | Trypanosomatidae | 58% | 93% |
A0A3R7JX82 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WUP9 | Leishmania donovani | 33% | 99% |
A0A3S7X9I5 | Leishmania donovani | 86% | 94% |
A0A422P2S2 | Trypanosoma rangeli | 57% | 95% |
A4H9A7 | Leishmania braziliensis | 33% | 100% |
A4HXM7 | Leishmania infantum | 33% | 99% |
A4IBI3 | Leishmania infantum | 86% | 90% |
C9ZJ61 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 99% |
C9ZZ57 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 97% |
E9AFB9 | Leishmania major | 87% | 100% |
E9ARD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 99% |
E9B6H4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 94% |
Q4QE41 | Leishmania major | 33% | 100% |
V5B5M6 | Trypanosoma cruzi | 34% | 100% |
V5BY63 | Trypanosoma cruzi | 59% | 95% |